| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52552460-52552880 | Rare:171 | ||||
| chr1:52553055-52553850 | Common:13; Rare:323 | ||||
| chr1:52697900-52698240 | Common:5; Rare:151 | ||||
| chr1:52698256-52698487 | Common:5; Rare:141; Clinvar (pathogenic):2 | ||||
| chr1:52842490-52842990 | Common:9; Rare:249 | ||||
| chr1:52927207-52927321 | Common:2; Rare:36 | ||||
| chr1:53014700-53015010 | Rare:130 | ||||
| chr1:53196629-53196919 | Common:1; Rare:203; Clinvar:10; Clinvar (benign):2 | ||||
| chr1:53220560-53220763 | Common:4; Rare:166 | ||||
| chr1:53238448-53238695 | Common:4; Rare:156 | ||||
| chr1:53327936-53328245 | Common:2; Rare:133 | ||||
| chr1:53837910-53838361 | Common:6; Rare:171 | ||||
| chr1:53838427-53838708 | Rare:68 | ||||
| chr1:53889723-53889977 | Common:3; Rare:137 | ||||
| chr1:53945561-53946125 | Common:14; Rare:246 |